DSAART
6 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for DSAART and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-12-24FDA-DeviceClass IIStop using AART Calf Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
- 2025-12-24FDA-DeviceClass IIStop using AART Pectoral Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
- 2025-12-24FDA-DeviceClass IIStop using AART Malar Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
- 2025-12-24FDA-DeviceClass IIStop using AART Chin Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
- 2025-12-24FDA-DeviceClass IIStop using AART Gluteal Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
- 2025-12-24FDA-DeviceClass IIStop using AART Silicone Carving Implants
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
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